Canonical Allele Identifier: CA894254668
Gene:

Linked Data

dbSNP Id: rs1455469519
gnomAD v3: 2-88016340-T-C
gnomAD v4: 2-88016340-T-C
MyVariant Identifiers: chr2:g.88315859T>C (hg19) chr2:g.88016340T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016340T>C , CM000664.2:g.88016340T>C GRCh38
NC_000002.11:g.88315859T>C , CM000664.1:g.88315859T>C GRCh37
NC_000002.10:g.88096974T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.685T>C
XR_940336.3:n.685T>C
Search 100 bp 5'
Search 100 bp 3'